chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89105134	89105135	G	A	12	GENIC	homozygous	116675076
10	89107690	89107691	T	A	8	GENIC	homozygous	116675078
10	89107932	89107933	G	A	20	GENIC	homozygous	116675080
10	89109739	89109740	T	C	18	GENIC	homozygous	116675082
10	89116937	89116938	C	T	12	GENIC	homozygous	116675096
10	89116949	89116950	A	G	14	GENIC	homozygous	116675098
10	89121809	89121810	A	G	17	GENIC	homozygous	116675102
10	89124297	89124298	G	C	9	GENIC	homozygous	116675106
10	89124581	89124582	G	C	17	GENIC	homozygous	116675108
10	89125820	89125821	T	C	32	GENIC	homozygous	116675110
10	89127412	89127413	A	G	25	GENIC	homozygous	116675112
10	89127461	89127462	A	G	13	GENIC	homozygous	116675114
10	89130550	89130551	T	C	6	GENIC	homozygous	116675118
10	89130764	89130765	T	C	16	GENIC	homozygous	116675120
10	89130808	89130809	T	A	7	GENIC	homozygous	116902192
10	89112468	89112469	G	T	11	GENIC	homozygous	116902182
10	89123079	89123080	C	T	23	GENIC	homozygous	116902184
10	89123146	89123147	G	A	29	GENIC	homozygous	116902186
10	89128621	89128622	G	T	10	GENIC	homozygous	116902188
10	89130531	89130532	G	A	8	GENIC	homozygous	116902190
10	89131551	89131552	A	C	20	GENIC	homozygous	116675122
10	89132622	89132623	A	G	13	GENIC	homozygous	116675124
10	89132749	89132750	A	G	13	GENIC	homozygous	116675126
10	89133423	89133424	T	C	13	GENIC	homozygous	116902194
10	89133749	89133750	G	A	23	GENIC	homozygous	116902196